Certificate in MedTech Compliance for Researchers
-- ViewingNowThe Certificate in MedTech Compliance for Researchers is a comprehensive course designed to equip learners with the essential skills needed to navigate the complex regulatory landscape of the medical technology industry. This program emphasizes the importance of compliance in research and development, clinical trials, and product commercialization.
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โข Medical Device Regulations: Understanding legal frameworks and guidelines for medical devices, including FDA, EU MDR, and other international regulations
โข Quality Management Systems: Overview of ISO 13485 and its role in MedTech compliance
โข Clinical Research and Trials: Designing and conducting compliant clinical research and trials, including ICH-GCP guidelines
โข Clinical Data Management: Best practices for managing, analyzing, and reporting clinical data to ensure compliance
โข Risk Management: Implementing risk management strategies in MedTech research, including ISO 14971 and FMEA
โข Labeling and Packaging: Ensuring compliant labeling and packaging, including UDI and IFU requirements
โข Post-Market Surveillance: Monitoring and reporting adverse events, including MDR submissions and vigilance reporting
โข MedTech Ethics: Navigating ethical considerations in MedTech research, including informed consent and patient privacy
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